An adenovirus vector for gene transfer into neurons and glia in the brain.
about
CAR-associated vesicular transport of an adenovirus in motor neuron axonsThe AMPA receptor interacts with and signals through the protein tyrosine kinase LynGene therapy in the inner ear using adenovirus vectors.Imaging and recording subventricular zone progenitor cells in live tissue of postnatal miceIn vivo transgene expression from an adenoviral vector is altered following a 6-OHDA lesion of the dopamine system.Effective prevention of thrombocytopenia in mice using adenovirus-mediated transfer of HST-1 (FGF-4) geneEfficient generation of recombinant adenoviruses using adenovirus DNA-terminal protein complex and a cosmid bearing the full-length virus genome.Ectodomain of coxsackievirus and adenovirus receptor genetically fused to epidermal growth factor mediates adenovirus targeting to epidermal growth factor receptor-positive cells.Gene delivery to the spinal cord: comparison between lentiviral, adenoviral, and retroviral vector delivery systemsCharacterization of promoter function and cell-type-specific expression from viral vectors in the nervous system.In situ use of suicide genes for therapy of brain tumours.Gene transfer into rat brain using adenoviral vectors.Nonneurotropic adenovirus: a vector for gene transfer to the brain and gene therapy of neurological disordersCurrent status of viral gene therapy for brain tumours.Gene therapy in human cancer: report of human clinical trials.Gene therapy for Parkinson's disease: review and update.Low-efficiency of percutaneous adenovirus-mediated arterial gene transfer in the atherosclerotic rabbitFrom gene transfer to gene therapy in lysosomal storage diseases affecting the central nervous system.Versatile somatic gene transfer for modeling neurodegenerative diseases.Regulation of excitatory transmission at hippocampal synapses by calbindin D28k.Approaches for gene delivery to the subfornical organ and magnocellular neurons.The protein kinase Mζ network as a bistable switch to store neuronal memory.Use of genetically engineered mice in drug discovery and development: wielding Occam's razor to prune the product portfolio.Cellular and humoral immune responses to adenoviral vectors containing factor IX gene: tolerization of factor IX and vector antigens allows for long-term expressionRetroviral-mediated gene transfer corrects very-long-chain fatty acid metabolism in adrenoleukodystrophy fibroblasts.The Himar1 mariner transposase cloned in a recombinant adenovirus vector is functional in mammalian cellsPreferential and bidirectional labeling of the rubrospinal tract with adenovirus-GFP for monitoring normal and injured axons.Comparison of the efficacy of four viral vectors for transducing hypothalamic magnocellular neurosecretory neurons in the rat supraoptic nucleusGene therapy for cerebral vascular disease: update 2003.Krox-20 patterns the hindbrain through both cell-autonomous and non cell-autonomous mechanismsReversible demyelination, blood-brain barrier breakdown, and pronounced neutrophil recruitment induced by chronic IL-1 expression in the brain.Gene therapy for brain tumors: regression of experimental gliomas by adenovirus-mediated gene transfer in vivo.Peripheral infection with adenovirus causes unexpected long-term brain inflammation in animals injected intracranially with first-generation, but not with high-capacity, adenovirus vectors: toward realistic long-term neurological gene therapy for chCellular immunity to viral antigens limits E1-deleted adenoviruses for gene therapyPreproenkephalin promoter yields region-specific and long-term expression in adult brain after direct in vivo gene transfer via a defective herpes simplex viral vector.Apolipoprotein E deficiency in mice: gene replacement and prevention of atherosclerosis using adenovirus vectorsComparison of intracerebral inoculation and osmotic blood-brain barrier disruption for delivery of adenovirus, herpesvirus, and iron oxide particles to normal rat brain.Endothelial cell implantation and survival within experimental gliomas.Site-specific recombination mediated by an adenovirus vector expressing the Cre recombinase protein: a molecular switch for control of gene expression.Lack of evidence of phenotypic complementation of E1A/E1B-deleted adenovirus type 5 upon superinfection by wild-type virus in the cotton rat.
P2860
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P2860
An adenovirus vector for gene transfer into neurons and glia in the brain.
description
1993 nî lūn-bûn
@nan
1993年の論文
@ja
1993年学术文章
@wuu
1993年学术文章
@zh
1993年学术文章
@zh-cn
1993年学术文章
@zh-hans
1993年学术文章
@zh-my
1993年学术文章
@zh-sg
1993年學術文章
@yue
1993年學術文章
@zh-hant
name
An adenovirus vector for gene transfer into neurons and glia in the brain.
@en
An adenovirus vector for gene transfer into neurons and glia in the brain.
@nl
type
label
An adenovirus vector for gene transfer into neurons and glia in the brain.
@en
An adenovirus vector for gene transfer into neurons and glia in the brain.
@nl
prefLabel
An adenovirus vector for gene transfer into neurons and glia in the brain.
@en
An adenovirus vector for gene transfer into neurons and glia in the brain.
@nl
P2093
P2860
P356
P1433
P1476
An adenovirus vector for gene transfer into neurons and glia in the brain.
@en
P2093
Le Gal La Salle G
Stratford-Perricaudet LD
P2860
P304
P356
10.1126/SCIENCE.8382374
P407
P577
1993-02-01T00:00:00Z